124 research outputs found

    Nuclear gamma resonance of Sn119 and Fe57 in franckeite and cylindrite.

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    The NGR data indicate that the coordination symmetry and valence states of tin ions are the same in franckeite and cylindrite, but that cylindrite contains more Sn2+. Also Fe is essential to both minerals. Apparently one structural layer in both minerals contains Fe ions combined with disulphide groups S-S2-, and the other layer is composed of FeS6 octahedra. -K.A.R

    Application of nuclear quadrupole resonance in study of minerals

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    The NQR method has been used to study some structural and chemical properties of minerals that are difficult or impossible to determine by conventional methods. For example, an X-ray determination commonly integrates the data for all cells, whereas NQR can separate the nearly ideal from highly distorted ones. It can thus give a better picture of the ideal structure and can determine the "degree of defectiveness." The method also has a very high sensitivity for crystallochemical effects. In this connection it has shown that arsenic selenide and orpiment are not strictly isostructural, as was previously thought. Nuclear magnetic resonance and NQR have been particularly successful in order-disorder studies. The latter can also be used as a rapid method of mineral identification. There are important restrictions on mineralogical applications, however: 1) compounds studied must have isotopes with nuclei that carry quadrupole moments; 2) symmetry at the sites of these nuclei must be lower than cubic; 3) concentration of atoms must be about 106 times higher than for the electron paramagnetic resonance method.-E. Ingerson. © 1967 Taylor & Francis Group, LLC

    Ultracold scattering processes in three-atomic helium systems

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    We review results on scattering observables for 4^4He--4^4He2_2 and 3^3He--4^4He2_2 collisions. We also study the effect of varying the coupling constant of the atom-atom interaction on the scattering length

    Structure and transport properties of stephanite (Ag 5SbS 4) according to antimony nuclear quadrupole resonance

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    Silver sulfo-antimonide Ag 5SbS 4 (stephanite) has been studied by nuclear quadrupole resonance (NQR) spectroscopy on antimony nuclei. The temperature dependences of the spectroscopic and relaxation parameters have been examined in the range of 4. 2-395 K. A phase transition at 140 K and internal motions with an activation energy of 0. 29 eV have been experimentally detected. The nature of the phase transition and diffusion of silver ions has been discussed in view of the reported data. © 2012 Pleiades Publishing, Ltd

    Electronic structure and indirect spin-spin interactions in bournonite (CuPbSbS3) according to antimony nuclear quadrupole resonance

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    A complex sulfide CuPbSbS3 (bournonite) has been studied by the nuclear quadrupole resonance on 121,123Sb. The temperature dependences of the spectroscopic and relaxation parameters in the temperature range of 10-295 K have been obtained. The crystallochemical features of the environment of the two non-equivalent Sb positions in the unit cell have been revealed from the nuclear quadrupole resonance spectra. The existence of the lattice vibrations with the frequency ω = 110 cm-1 has been demonstrated on the basis of the temperature dependence of the nuclear quadrupole resonance frequencies. Slow beats have been observed on the decay curve of the spin echo signal. Experimental data have been analyzed in order to reveal the existence of the indirect spin-spin interactions involving Sb atoms. The indirect spin-spin coupling constant has been estimated as J = 2.5 ± 0.5 kHz. © 2013 Pleiades Publishing, Ltd

    A novel data on Ag5SbS4 and CuPbSbS3 probed by antimony NQR spectroscopy

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    Investigations of Sb-based chalcogenides, stephanite Ag5SbS 4 and bournonite CuPbSbS 3, have been performed by 121,123Sb nuclear quadrupole resonance (NQR). In stephanite a phase transition at 140 K and internal diffusion motions with an activation energy of 0.29 eV have been experimentally detected. The analysis of experimental results for bournonite revealed two crystal-chemical positions of Sb in the unit cell with distinct local symmetry. The NQR frequencies ν and line-widths Δν data indicate that Sb(A)S3 complex has almost axial symmetry, but Sb(B)S 3 complex is substantially distorted

    Copper valence, structural separation and lattice dynamics in tennantite (fahlore): NMR, NQR and SQUID studies

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    Electronic and magnetic properties of tennantite subfamily of tetrahedrite-group minerals have been studied by copper nuclear quadrupole resonance (NQR), nuclear magnetic resonance (NMR) and SQUID magnetometry methods. The temperature dependences of copper NQR frequencies and line-width, nuclear spin-lattice relaxation rate T1 -1 and nuclear spin-echo decay rate T2 -1 in tennantite samples in the temperature range 4.2-210 K is evidence of the presence of field fluctuations caused by electronic spins hopping between copper CuS3 positions via S2 bridging atom. The analysis of copper NQR data at low temperatures points to the magnetic phase transition near 65 K. The magnetic susceptibility in the range 2-300 K shows a Curie-Weiss behavior, which is mainly determined by Fe2+ paramagnetic substituting ions. © Springer-Verlag 2007

    Oxidation and magnetic states of chalcopyrite CuFeS2: A first principles calculation

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    The ground state band structure, magnetic moments, charges and population numbers of electronic shells of Cu and Fe atoms have been calculated for chalcopyrite CuFeS2 using density functional theory. The comparison between our calculation results and experimental data (X-ray photoemission, X-ray absorption and neutron diffraction spectroscopy) has been made. Our calculations predict a formal oxidation state for chalcopyrite as Cu 1+Fe3+S2 2-. However, the assignment of formal valence state to transition metal atoms appears to be oversimplified. It is anticipated that the valence state can be confirmed experimentally by nuclear magnetic and nuclear quadrupole resonance and Mössbauer spectroscopy methods. © 2014 Pleiades Publishing, Ltd

    Contribution of copper Nqr spectroscopy to the geological studies of complex sulfides and oxides

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    Many energy-related areas such as nuclear waste isolation, continental drilling, fossil fuel recovery, and geothermal energy are directly associated with an in-depth understanding of the earth sciences. Of particular interest is the development of analytical techniques which can augment existing ones in developing a better understanding of mineralogy. Presently, available instrumental techniques for studying mineralogical problems such as x-ray, electron and neutron diffraction, nuclear gamma resonance (NGR or Mössbauer spectroscopy), electron microscopy and transmission electron microscopy have inherent limitations. These manifest themselves in being unable to characterize mineral samples fully, especially if they are polycrystalline. Nuclear Quadrupole Resonance (NQR) spectroscopy offers the potential for being able to obtain accurate high resolution spectra. These can then be interpreted to give structural information which can be related to local electronic structure, atomic arrangement, order/disorder phenomena, and crystal phase transformation. In addition, internal dynamics (ionic diffusion, metallic behavior, rotations, and so on) in the solid state can be studied. Furthermore, since NQR data are sensitive to changes in temperature and pressure, there is the possibility of obtaining stress/strain information. As applied to mineralogical and geological problems, NQR can also provide additional information, for example: chemical activity of minerals (genetic and technological aspects) at different hydrothermal conditions, the studies of impurity configurations in ore minerals and their distribution in crystal lattice, and other. This chapter highlights some NQR studies in copper sulfides, which demonstrate how NQR method can contribute to our understanding of geological problems. Examples are taken primarily from author's investigate groups. © 2009 Springer Science+Business Media B.V
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